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Cannarelief 1000mg - Medication Information

Product NDC Code 82876-010
Drug Name

Cannarelief 1000mg

Type Brand
Active Ingredients
Menthol 7.9 g/71.9g
Route TOPICAL
Dosage Form SALVE
Application Number part348
Labeler Name Carolina Cannabis Creations LLC
Packages
Package NDC Code Description
82876-010-49 71.9 g in 1 tube (82876-010-49)
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Overdosage of Cannarelief 1000mg

Information about signs, symptoms, and laboratory findings of acute ovedosage and the general principles of overdose treatment.
In case of an overdose seek medical help or contact a poison control center right away

Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active Ingredients Menthol...........11.3% Purpose Menthol 11.3%.........................Topical Analgesic Purpose Menthol 11.3%.........................Topical Analgesic

Dosage and administration

Information about the drug product’s dosage and administration recommendations, including starting dose, dose range, titration regimens, and any other clinically sigificant information that affects dosing recommendations.
Directions Adults and children 12 years and over; apply to the affected area one to four times daily Children 12 years and younger; ask a doctor Keep out of reach of children keep out of reach of children Keep out of reach of children keep out of reach of children

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients Arnica Montana oil, Arrowroot powder, Beeswax, Cannabidiol, Coconut oil, Rice bran oil, Rosemary oil, and Shea butter.

Indications and usage

A statement of each of the drug products indications for use, such as for the treatment, prevention, mitigation, cure, or diagnosis of a disease or condition, or of a manifestation of a recognized disease or condition, or for the relief of symptoms associated with a recognized disease or condition. This field may also describe any relevant limitations of use.
Uses Temporary relief of aches and pains associated with arthritis, backache, joint pain, muscle strains, and sprains

Purpose

Information about the drug product’s indications for use.
Purpose Menthol 11.3%.........................Topical Analgesic Purpose Menthol 11.3%.........................Topical Analgesic

Spl product data elements

Usually a list of ingredients in a drug product.
Cannarelief 1000mg Menthol JOJOBA OIL PEG-8 BEESWAX COCONUT OIL MENTHOL MENTHOL ROSEMARY OIL RICE BRAN OIL SHEA BUTTER CANNABIDIOL ARNICA MONTANA FLOWER WATER MARANTA ARUNDINACEA ROOT

Package label principal display panel

The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.
Front label front label Back label back label

Ask doctor

Information about when a doctor should be consulted about existing conditions or sumptoms before using the drug product, including all warnings for persons with certain preexisting conditions (excluding pregnancy) and all warnings for persons experiencing certain symptoms. The warnings under this heading are those intended only for situations in which consumers should not use the product until a doctor is consulted.
Stop use and ask a doctor if Condition worsens, Symptoms last more than 7 days, Condition clears up but occurs again within a few days, Rash or irritations occurs

Keep out of reach of children

Information pertaining to whether the product should be kept out of the reach of children, and instructions about what to do in the case of accidental contact or ingestion, if appropriate.
Keep out of reach of children keep out of reach of children Keep out of reach of children keep out of reach of children

Other safety information

Information about safe use and handling of the product that may not have been specified in another field.
Other information Store at 68-77 degrees F, Avoid direct sunlight

Stop use

Information about when use of the drug product should be discontinued immediately and a doctor consulted. Includes information about any signs of toxicity or other reactions that would necessitate immediately discontinuing use of the product.
Stop use and ask a doctor if The condition worsens, symptoms last more than 7 days, the condition clears but occurs again within a few days, Rash or irritation occurs Stop use and ask a doctor if Condition worsens, Symptoms last more than 7 days, Condition clears up but occurs again within a few days, Rash or irritations occurs

When using

Information about side effects that people may experience, and the substances (e.g. alcohol) or activities (e.g. operating machinery, driving a car) to avoid while using the drug product.
When using this product Do not apply to wounds or irritated skin, and avoid contact with eyes

Pregnancy or breast feeding

Pregnancy or Breast feeding
If pregnant or breastfeeding Consult a health professional before use In case of an overdose seek medical help or contact a poison control center right away

Warnings

Information about serious adverse reactions and potential safety hazards, including limitations in use imposed by those hazards and steps that should be taken if they occur.
Warnings FOR EXTERNAL USE ONLY, provides penetrating pain relief

Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API